Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58343Generated: October 25, 2026

1,1'-Carbonyldiimidazole → 8,8,11,14,14-Pentamethyl-7,12-dioxo-1,1,1-triphenyl-13-oxa-6,11-diaza-1-phosphoniapentadecane bromide

https://huagongshe.com/reaction/58343

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant(4-Aminobutyl)(triphenyl)phosphonium bromideHCID 10201848—
Reactant4-[(Tert-butoxycarbonyl)(methyl)amino]-2,2-dimethylbutanoic acidHCID 54754482—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product8,8,11,14,14-Pentamethyl-7,12-dioxo-1,1,1-triphenyl-13-oxa-6,11-diaza-1-phosphoniapentadecane bromideHCID 8946336869%

Reaction Steps

4-[(tert-butoxycarbonyl)(methyl)amino]-2,2-dimethylbutanoic acid (Organic and Molecular Chemistry, 2011, 9, 1846-1854, 117 mg, 0.48 mmol) was dissolved in N,N-dimethylformamide (1.2 mL) and treated with N,N-carbonyldiimidazole (104 mg, 0.64 mmol). The mixture was stirred at room temperature for 30 minutes. (4-Aminobutyl)(triphenyl)phosphonium bromide (277 mg, 0.67 mmol) was added, and the reaction was stirred overnight at room temperature. The reaction mixture was then diluted with methylene chloride and washed with 5% aqueous lithium chloride (3 times), 1N aqueous hydrogen chloride, and saturated sodium bicarbonate. The organic solution was dried over anhydrous sodium sulfate, filtered, and concentrated to give the title compound (210 mg, 69%) as a white foam. Sample was used crude in next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434753B2
Source datasetuspto-grants-2016_09
ORD IDord-b462afc41980416ea4c8e455f09a0e8c
Source noteuspto-grants-2016_09